Variant #0000655487 (NC_000006.11:g.135787520A>G, NC_000006.11(NM_001134831.1):c.190-9T>C (AHI1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135787520A>G
DNA change (hg38) g.135466382A>G
Published as AHI1(NM_001350503.1):c.190-9T>C
ISCN -
DB-ID AHI1_000120
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AHI1 NM_001134831.1 -?/. - c.190-9T>C r.(=) p.(=)
AHI1 NM_017651.4 -?/. - c.190-9T>C r.(=) p.(=)


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